WO2006003500A8 - Method for preparing 5-`4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3h`1,2,4!triazin-2-yl!-benzamide derivatives by deprotecting the hydroxyl-protected precursers - Google Patents

Method for preparing 5-`4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3h`1,2,4!triazin-2-yl!-benzamide derivatives by deprotecting the hydroxyl-protected precursers

Info

Publication number
WO2006003500A8
WO2006003500A8 PCT/IB2005/002036 IB2005002036W WO2006003500A8 WO 2006003500 A8 WO2006003500 A8 WO 2006003500A8 IB 2005002036 W IB2005002036 W IB 2005002036W WO 2006003500 A8 WO2006003500 A8 WO 2006003500A8
Authority
WO
WIPO (PCT)
Prior art keywords
preparing
precursers
triazin
deprotecting
dioxo
Prior art date
Application number
PCT/IB2005/002036
Other languages
French (fr)
Other versions
WO2006003500A1 (en
Inventor
Zhengong B Li
Original Assignee
Pfizer Prod Inc
Zhengong B Li
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34972172&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2006003500(A8) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer Prod Inc, Zhengong B Li filed Critical Pfizer Prod Inc
Priority to MXPA06014022A priority Critical patent/MXPA06014022A/en
Priority to EP05757546A priority patent/EP1776352A1/en
Priority to AU2005258911A priority patent/AU2005258911A1/en
Priority to JP2007518730A priority patent/JP2008504360A/en
Priority to BRPI0512781-5A priority patent/BRPI0512781A/en
Priority to CA002571124A priority patent/CA2571124A1/en
Publication of WO2006003500A1 publication Critical patent/WO2006003500A1/en
Publication of WO2006003500A8 publication Critical patent/WO2006003500A8/en
Priority to NO20065327A priority patent/NO20065327L/en
Priority to IL179461A priority patent/IL179461A0/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D253/00Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
    • C07D253/02Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
    • C07D253/061,2,4-Triazines
    • C07D253/0651,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members
    • C07D253/071,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members with hetero atoms, or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D253/075Two hetero atoms, in positions 3 and 5
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis

Abstract

The present invention relates to the methods for preparing compounds of the formula (I): or the pharmaceutically acceptable salts thereof, wherein R1, R2, R4, R10, and R11 have any of the values defined in the specification. The compounds of the present invention are useful in the treatment of diseases, including inflammatory diseases such as rheumatoid arthritis.
PCT/IB2005/002036 2004-06-29 2005-06-16 Method for preparing 5-`4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3h`1,2,4!triazin-2-yl!-benzamide derivatives by deprotecting the hydroxyl-protected precursers WO2006003500A1 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
MXPA06014022A MXPA06014022A (en) 2004-06-29 2005-06-16 Methods for preparing p2x7 inhibitors.
EP05757546A EP1776352A1 (en) 2004-06-29 2005-06-16 Method for preparing 5-[4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3h[1,2,4]triazin-2-yl]-benzamide derivatives by deprotecting the hydroxyl-protected precursers
AU2005258911A AU2005258911A1 (en) 2004-06-29 2005-06-16 Method for preparing 5-`4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3H`1,2,4!triazin-2-YL!-benzamide derivatives by deprotecting the hydroxyl-protected precursers
JP2007518730A JP2008504360A (en) 2004-06-29 2005-06-16 5- [4- (2-hydroxy-propyl) -3,5-dioxo-4,5-dihydro-3H-1,2,4-triazin-2-yl by deprotecting the hydroxyl protected precursor Method for producing benzamide derivative
BRPI0512781-5A BRPI0512781A (en) 2004-06-29 2005-06-16 Method for preparing 5- {4- (2-hydroxy-propyl) -3,5-dioxo-4,5-dihydro-3h- [1,2,4] triazin-2-yl} -benzamide derivatives by of the unprotection of hydroxyl protector precursors
CA002571124A CA2571124A1 (en) 2004-06-29 2005-06-16 Method for preparing 5-`4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3h`1,2,4!triazin-2-yl!-benzamide derivatives by deprotecting the hydroxyl-protected precursers
NO20065327A NO20065327L (en) 2004-06-29 2006-11-20 Process for the preparation of derivatives of 5- [4- (2-hydroxy-propyl) -3,5-dihydro-3H'1, 2,4 (triazin-2-yl) -benzamide.
IL179461A IL179461A0 (en) 2004-06-29 2006-11-21 Method for preparing 5-[4-(2-hydroxy-propyl)-3,5-dioxo-4,5,-dihydro-3h] 2,4-[triazin-2-yl]-benzamide derivatives by deprotecting the hydroxyl-protected precursers

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US58385104P 2004-06-29 2004-06-29
US60/583,851 2004-06-29

Publications (2)

Publication Number Publication Date
WO2006003500A1 WO2006003500A1 (en) 2006-01-12
WO2006003500A8 true WO2006003500A8 (en) 2006-04-13

Family

ID=34972172

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2005/002036 WO2006003500A1 (en) 2004-06-29 2005-06-16 Method for preparing 5-`4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3h`1,2,4!triazin-2-yl!-benzamide derivatives by deprotecting the hydroxyl-protected precursers

Country Status (15)

Country Link
US (1) US7235657B2 (en)
EP (1) EP1776352A1 (en)
JP (1) JP2008504360A (en)
CN (1) CN1980902A (en)
AR (1) AR049653A1 (en)
AU (1) AU2005258911A1 (en)
BR (1) BRPI0512781A (en)
CA (1) CA2571124A1 (en)
IL (1) IL179461A0 (en)
MX (1) MXPA06014022A (en)
NO (1) NO20065327L (en)
RU (1) RU2006146675A (en)
TW (1) TW200612964A (en)
WO (1) WO2006003500A1 (en)
ZA (1) ZA200609579B (en)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU228426B1 (en) 1996-07-24 2013-03-28 Warner Lambert Co Use of isobutylgaba and its derivatives for the preparation of pharmaceuticals for treating pain
PA8557501A1 (en) 2001-11-12 2003-06-30 Pfizer Prod Inc BENZAMIDA, HETEROARILAMIDA AND INVESTED AMIDAS
PA8591801A1 (en) * 2002-12-31 2004-07-26 Pfizer Prod Inc BENZAMID INHIBITORS OF THE P2X7 RECEIVER.
DE602004005033T2 (en) 2003-05-12 2007-08-09 Pfizer Products Inc., Groton BENZAMIDINHIBITORS OF THE P2X7 RECEPTOR
US8232290B2 (en) 2008-03-25 2012-07-31 Affectis Pharmaceuticals Ag P2X7R antagonists and their use
JP2010043063A (en) * 2008-05-09 2010-02-25 Agency For Science Technology & Research Diagnosis and treatment of kawasaki disease
PT2243772E (en) 2009-04-14 2012-03-28 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
EP2322149A1 (en) 2009-11-03 2011-05-18 Universidad del Pais Vasco Methods and compositions for the treatment of ischemia
BR112012028850A2 (en) 2010-05-14 2015-09-15 Affectis Pharmaceuticals Ag methods for preparing p2x7r antagonists
WO2012110190A1 (en) 2011-02-17 2012-08-23 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
WO2012163456A1 (en) 2011-05-27 2012-12-06 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
WO2012163792A1 (en) 2011-05-27 2012-12-06 Affectis Pharmaceuticals Ag Novel p2x7r antagonists and their use
US9988373B2 (en) 2013-12-26 2018-06-05 Shionogi & Co., Ltd. Nitrogen-containing six-membered cyclic derivatives and pharmaceutical composition comprising the same
EP3957627A1 (en) * 2015-04-24 2022-02-23 Shionogi & Co., Ltd 6-membered heterocyclic derivative and pharmaceutical composition comprising same
WO2017209265A1 (en) * 2016-06-03 2017-12-07 塩野義製薬株式会社 Bicyclic heterocyclic derivative and pharmaceutical composition containing same
WO2018074390A1 (en) 2016-10-17 2018-04-26 塩野義製薬株式会社 Bicyclic nitrogenated heterocyclic derivative and pharmaceutical composition containing same
JP6692113B2 (en) * 2016-10-21 2020-05-13 塩野義製薬株式会社 Pharmaceutical composition containing 6-membered heterocyclic derivative

Family Cites Families (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4318731A (en) 1979-08-25 1982-03-09 Nihon Nohyaku Co., Ltd. Δ2 -1,2,4-triazolin-5-one derivatives and herbicidal usage thereof
AU542544B2 (en) 1980-03-12 1985-02-28 Nippon Kayaku Kabushiki Kaisha Tetrahydrophthalimide derivatives
EP0077938A3 (en) 1981-10-23 1983-08-24 Mitsubishi Kasei Corporation N-(3-substituted aminophenyl) tetrahydrophthalimides and herbicidal composition
GR80558B (en) 1983-10-08 1985-02-06 Nippon Kayaku Kk Derivative of pyrazole and use thereof as a herbicide
US4766233A (en) 1984-06-12 1988-08-23 Fmc Corporation Herbicidal 2-aryl-1,2,4-triazine-3,5(2H,4H)-diones and sulfur analogs thereof
AU578708B2 (en) 1984-06-12 1988-11-03 Fmc Corporation Herbicidal 2-aryl-1,2,4-triazine-3,5(2h,4h)-diones and sulfuranalogs thereof
US4806145A (en) 1984-10-31 1989-02-21 Fmc Corporation Herbicidal aryl triazolinones
JPS6299368A (en) 1985-10-26 1987-05-08 Nippon Nohyaku Co Ltd Delta2-1,2,4-triazolin-5-one derivative production and use thereof
HU203542B (en) 1987-09-23 1991-08-28 Hoffmann La Roche Herbicide compositions containing pyrimidinyl-benzamide derivatives and process for producing the active components
US5411980A (en) 1989-07-28 1995-05-02 Merck & Co., Inc. Substituted triazolinones, triazolinethiones, and triazolinimines as angiotensin II antagonists
US5077409A (en) 1990-05-04 1991-12-31 American Cyanamid Company Method of preparing bis-aryl amide and urea antagonists of platelet activating factor
US5128351A (en) 1990-05-04 1992-07-07 American Cyanamid Company Bis-aryl amide and urea antagonists of platelet activating factor
KR930703259A (en) 1990-12-17 1993-11-29 알베르투스 빌헬무스 요아네스 쩨스트라텐 Disinfectant Isoquinoline Derivatives
JP3089621B2 (en) 1990-12-17 2000-09-18 日産化学工業株式会社 Uracil derivatives
WO1992020662A1 (en) 1991-05-10 1992-11-26 Merck & Co., Inc. Acidic aralkyl triazole derivatives active as angiotensin ii antagonists
GB9110679D0 (en) 1991-05-17 1991-07-10 Sandoz Ltd Improvements in or relating to organic compounds
GB9119467D0 (en) 1991-09-12 1991-10-23 Smithkline Beecham Corp Chemical compounds
DE4405614A1 (en) 1994-02-22 1995-08-24 Bayer Ag Substituted triazolinones
US5686061A (en) 1994-04-11 1997-11-11 The Board Of Regents Of The University Of Texas System Particulate contrast media derived from non-ionic water soluble contrast agents for CT enhancement of hepatic tumors
GB9412603D0 (en) 1994-06-23 1994-08-10 Sandoz Ltd Organic compounds
HRP950330A2 (en) 1994-07-05 1997-10-31 Ciba Geigy Ag New herbicides
US6001862A (en) 1995-06-02 1999-12-14 Kyorin Pharameuticals Co., Ltd. N-benzyldioxothiazolidylbenzamide derivatives and processes for preparing the same
US6147101A (en) 1995-06-02 2000-11-14 Kyorin Pharmaceutical Co., Ltd. N-benzyldioxothiazolidylbenzamide derivatives and process for producing the same
JP3144624B2 (en) 1995-06-02 2001-03-12 杏林製薬株式会社 N-benzyldioxothiazolidylbenzamide derivative and method for producing the same
JP3906935B2 (en) 1995-12-18 2007-04-18 杏林製薬株式会社 N-substituted dioxothiazolidylbenzamide derivative and process for producing the same
US5939418A (en) 1995-12-21 1999-08-17 The Dupont Merck Pharmaceutical Company Isoxazoline, isothiazoline and pyrazoline factor Xa inhibitors
DK0889877T3 (en) 1996-03-29 2001-10-01 Searle & Co Meta-substituted phenylene derivatives and their use as alpha-beta3 integrin antagonists or inhibitors
US6020357A (en) 1996-12-23 2000-02-01 Dupont Pharmaceuticals Company Nitrogen containing heteroaromatics as factor Xa inhibitors
ATE443698T1 (en) 1996-12-23 2009-10-15 Bristol Myers Squibb Pharma Co NITROGEN-CONTAINING HETEROCYCLES AS FACTOR XA INHIBITORS
US6187797B1 (en) 1996-12-23 2001-02-13 Dupont Pharmaceuticals Company Phenyl-isoxazoles as factor XA Inhibitors
DE19701287A1 (en) 1997-01-16 1998-07-23 Wernicke & Co Gmbh Process for increasing the service life of grinding wheels
EP1019375A1 (en) 1997-03-25 2000-07-19 Astra Pharmaceuticals Limited Novel pyridine derivatives and pharmaceutical compositions containing them
DE19719621A1 (en) 1997-05-09 1998-11-12 Hoechst Ag Sulfonylaminocarboxylic acids
US6297239B1 (en) 1997-10-08 2001-10-02 Merck & Co., Inc. Inhibitors of prenyl-protein transferase
SE9704272D0 (en) 1997-11-21 1997-11-21 Astra Pharma Prod Novel Compounds
SE9704546D0 (en) 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
SE9704545D0 (en) 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
SE9704544D0 (en) 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
JPH11318492A (en) 1998-03-09 1999-11-24 Aisin Seiki Co Ltd Composition containing fluorogenic substrate
US6320078B1 (en) 1998-07-24 2001-11-20 Mitsui Chemicals, Inc. Method of producing benzamide derivatives
FR2783519B1 (en) 1998-09-23 2003-01-24 Sod Conseils Rech Applic NOVEL AMIDINE DERIVATIVES, THEIR PREPARATION, THEIR USE AS MEDICAMENTS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
DE19851184A1 (en) 1998-11-06 2000-05-11 Aventis Pharma Gmbh N-arylsulfonylamino acid omega amides
CA2355161A1 (en) 1998-12-16 2000-06-22 Bayer Aktiengesellschaft Biphenyl and biphenyl-analogous compounds as integrin antagonists
RU2254333C2 (en) 1999-04-09 2005-06-20 Астразенека Аб Derivatives of adamantane, method for their preparing, pharmaceutical composition based on thereof and methods for treatment
CA2382751A1 (en) 1999-05-24 2000-11-30 Cor Therapeutics, Inc. Inhibitors of factor xa
SE9901875D0 (en) 1999-05-25 1999-05-25 Astra Pharma Prod Novel compounds
EP1088821A1 (en) 1999-09-28 2001-04-04 Applied Research Systems ARS Holding N.V. Pharmaceutically active sulfonamide derivatives
EP1226112A4 (en) 1999-10-18 2004-10-13 Univ Connecticut Retro-anandamides, high affinity and stability cannabinoid receptor ligands
SE9904505D0 (en) 1999-12-09 1999-12-09 Astra Pharma Prod Novel compounds
SE9904652D0 (en) 1999-12-17 1999-12-17 Astra Pharma Prod Novel Compounds
TWI258462B (en) 1999-12-17 2006-07-21 Astrazeneca Ab Adamantane derivative compounds, process for preparing the same and pharmaceutical composition comprising the same
SE9904738D0 (en) 1999-12-22 1999-12-22 Astra Pharma Prod Novel compounds
DE10005284A1 (en) 2000-02-07 2001-08-09 Bayer Ag 1-Amino-3-phenyl-uracil preparation in high yield, for use as agrochemical or intermediate, by aminating 3-phenyl-uracil with 2-aminooxysulfonyl-1,3,5-trimethylbenzene
PT1226127E (en) 2000-05-04 2009-07-23 Basf Se Substituted phenyl sulfamoyl carboxamides
ATE440096T1 (en) 2000-12-08 2009-09-15 Takeda Pharmaceutical SUBSTITUTED THIAZOLE DERIVATIVES WITH 3-PYRIDYL GROUPS, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE
WO2003042190A1 (en) * 2001-11-12 2003-05-22 Pfizer Products Inc. N-alkyl-adamantyl derivatives as p2x7-receptor antagonists
PA8557501A1 (en) 2001-11-12 2003-06-30 Pfizer Prod Inc BENZAMIDA, HETEROARILAMIDA AND INVESTED AMIDAS
PA8591801A1 (en) * 2002-12-31 2004-07-26 Pfizer Prod Inc BENZAMID INHIBITORS OF THE P2X7 RECEIVER.
AU2003288640A1 (en) 2002-12-31 2004-07-22 Pfizer Products Inc. Benzamide inhibitors of the p2x7 receptor
DE602004005033T2 (en) 2003-05-12 2007-08-09 Pfizer Products Inc., Groton BENZAMIDINHIBITORS OF THE P2X7 RECEPTOR

Also Published As

Publication number Publication date
BRPI0512781A (en) 2008-04-08
EP1776352A1 (en) 2007-04-25
NO20065327L (en) 2006-12-18
WO2006003500A1 (en) 2006-01-12
ZA200609579B (en) 2008-08-27
TW200612964A (en) 2006-05-01
MXPA06014022A (en) 2007-02-08
RU2006146675A (en) 2008-07-10
CN1980902A (en) 2007-06-13
US20050288256A1 (en) 2005-12-29
US7235657B2 (en) 2007-06-26
AR049653A1 (en) 2006-08-23
IL179461A0 (en) 2007-05-15
AU2005258911A1 (en) 2006-01-12
JP2008504360A (en) 2008-02-14
CA2571124A1 (en) 2006-01-12

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